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Genome Medicine|December 5, 2014
Whole-genome haplotyping approaches and genomic medicineGustavo Glusman, Hannah C Cox, Jared C RoachHeadache|March 2, 2012
The role of the MTHFR gene in migraineShani Stuart, Hannah C Cox, Rod A Lea, et al.American Journal of Medical Genetics. Part A|February 27, 2025
Phenotypic Characteristics of a Patient Cohort With Recessive Dystrophic Epidermolysis Bullosa and the Pathogenic Variant c.7485+5G>A in Intron 98 of COL7A1Micah G Pascual, Hannah C Cox, Austin Larson, et al.Journal of Community Genetics|June 29, 2021
Demographic and socioeconomic trends in DNA banking utilization in the USAJoshua Prudent, Esthermarie Lopez, Donna Dorshorst, et al.Journal of Oncology Practice|January 14, 2017
Impact of Payer Constraints on Access to Genetic TestingPat Whitworth, Peter Beitsch, Christopher Arnell, et al.Cancer Genetics|March 11, 2017
Detection of somatic variants in peripheral blood lymphocytes using a next generation sequencing multigene pan cancer panelBradford Coffee, Hannah C Cox, John Kidd, et al.The Journal of Headache and Pain|October 28, 2011
Variants in the human potassium channel gene (KCNN3) are associated with migraine in a high risk genetic isolateHannah C Cox, Rod A Lea, Claire Bellis, et al.Human Mutation|September 7, 2019
A substantial proportion of apparently heterozygous TP53 pathogenic variants detected with a next-generation sequencing hereditary pan-cancer panel are acquired somaticallyBradford Coffee, Hannah C Cox, Ryan Bernhisel, et al.Breast Cancer Research and Treatment|September 12, 2020
Family history of breast cancer in men with non-BRCA male breast cancer: implications for cancer risk counselingGregory S Calip, John Kidd, Ryan Bernhisel, et al.Human Heredity|April 3, 2009
Principal component and linkage analysis of cardiovascular risk traits in the Norfolk isolateHannah C Cox, Claire Bellis, Rod A Lea, et al.Pageof 3